Allele Registry

Canonical Allele Identifier: PA113103

Gene: PTS HGNC NCBI

ClinVar RCV:

RCV000000506

RCV000778305

ClinVar Variation:

477

HGVS (amino-acid)	Matching Registered Transcripts
NP_000308.1:p.Arg16Cys	CA114317 NM_000317.3:c.46C>T